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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884809copy number variation1nstd102humanBenign GRCh37 chr5: 14,871,559-14,872,659 , GRCh38.p12 chr5: 14,871,450-14,872,550 ANKH, UQCRBP3
    nsv3882705copy number variation1nstd102humanBenign GRCh37 chr5: 14,871,610-14,872,659 , GRCh38.p12 chr5: 14,871,501-14,872,550 ANKH, UQCRBP3
    nsv3874680copy number variation1nstd102humanBenign GRCh37 chr5: 14,872,063-14,872,659 , GRCh38.p12 chr5: 14,871,954-14,872,550 ANKH, UQCRBP3
    nsv3873748copy number variation1nstd102humanBenign GRCh37 chr5: 14,871,610-14,877,474 , GRCh38.p12 chr5: 14,871,501-14,877,365 ANKH, HNRNPKP5, 1 more genes
    nsv3879102copy number variation1nstd102humanBenign GRCh37 chr5: 14,871,745-14,877,474 , GRCh38.p12 chr5: 14,871,636-14,877,365 ANKH, UQCRBP3, 1 more genes
    nsv3914649copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397 ANKH, LOC105374666, 399 more genes
    nsv3887142copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091 ANKH, H3Y1, 381 more genes
    nsv3910712copy number variation1nstd102humanPathogenic NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394 ANKH, ROPN1L, 378 more genes
    nsv3924496copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010 ANKH, LOC105374678, 356 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 ANKH, LOC105374608, 351 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 ANKH, BASP1, 338 more genes
    nsv3881706copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-31,343,671 , GRCh38.p12 chr5: 25,329-31,343,564 ANKH, IRX2-DT, 339 more genes
    nsv3883796copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-30,672,798 , GRCh38.p12 chr5: 25,329-30,672,691 ANKH, H3P22, 335 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 ANKH, LOC105374649, 333 more genes
    nsv3912696copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-30,112,642 , GRCh38 chr5: 49,978-30,112,535 , NCBI36 chr5: 103,093-30,148,399 ANKH, OTULINL, 333 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 ANKH, OTULINL, 317 more genes
    nsv3916877copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-28,625,056 , GRCh37 chr5: 22,149-28,589,299 , GRCh38 chr5: 22,149-28,589,192 ANKH, CTD-2154B17.1, 313 more genes
    nsv3922865copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-28,429,241 , GRCh37 chr5: 22,149-28,429,348 , NCBI36 chr5: 75,149-28,465,105 ANKH, CCT6P2, 312 more genes
    nsv3916127copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-27,824,480 , GRCh37 chr5: 22,149-27,788,723 , GRCh38 chr5: 22,149-27,788,616 ANKH, LOC101929898, 310 more genes
    nsv3914997copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-27,611,270 , GRCh38 chr5: 22,149-27,611,163 , NCBI36 chr5: 75,149-27,647,027 ANKH, LINC02241, 309 more genes
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